ScholarIQanswers from OpenAlex & ORCID
Tsutomu Ogata
ResearcherPublications, citations & collaboration network
Tsutomu Ogata is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Tsutomu Ogata have?
ScholarIQindexed works
Tsutomu Ogata has 779 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Tsutomu Ogata have?
ScholarIQcitation count
Tsutomu Ogata has 21,553 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Tsutomu Ogata?
ScholarIQh-index
Tsutomu Ogata has an h-index of 68 in OpenAlex.
What is the i10-index of Tsutomu Ogata?
ScholarIQi10-index
Tsutomu Ogata has an i10-index of 384 in OpenAlex.
What is the ORCID of Tsutomu Ogata?
ScholarIQorcid
The ORCID for Tsutomu Ogata is on the source record.
What is the OpenAlex record for Tsutomu Ogata?
ScholarIQopenalex
The OpenAlex for Tsutomu Ogata is on the source record.
What are the most-cited papers on Tsutomu Ogata?
ScholarIQmost cited works
Rationale and study design of the Japan environment and children’s study (JECS)
Toshihiro Kawamoto, Hiroshi Nitta, Katsuyuki Murata, Eisaku Toda, Naoya Tsukamoto, Manabu Hasegawa, Zentaro Yamagata, Fujio Kayama, Reiko Kishi, Yukihiro Ohya, Hirohisa Saito, Haruhiko Sago, Makiko Okuyama, Tsutomu Ogata, Susumu Yokoya, Yuji Koresawa, Yasuyuki Shibata, Shoji F. Nakayama, Takehiro Michikawa, Ayano Takeuchi, Hiroshi Satoh
Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes
Masayo Kagami, Yoichi Sekita, Gen Nishimura, Masahito Irie, Fumiko Kato, Michiyo Okada, Shunji Yamamori, Hiroshi Kishimoto, Masahiro Nakayama, Yukichi Tanaka, Kentarou Matsuoka, Tsutomu Takahashi, Mika Noguchi, Yoko Tanaka, Kouji Masumoto, Takeshi Utsunomiya, Hiroko Kouzan, Yumiko Komatsu, Hirofumi Ohashi, Kenji Kurosawa, Kenjirou Kosaki, Anne C. Ferguson‐Smith, Fumitoshi Ishino, Tsutomu Ogata
Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MEST
Masayo Kagami, Toshiro Nagai, Maki Fukami, Kazuki Yamazawa, Tsutomu Ogata
<i>MLL2</i> and <i>KDM6A</i> mutations in patients with Kabuki syndrome
Noriko Miyake, Eriko Koshimizu, Nobuhiko Okamoto, Seiji Mizuno, Tsutomu Ogata, Toshiro Nagai, Tomoki Kosho, Hirofumi Ohashi, Mitsuhiro Kato, Goro Sasaki, Hiroyo Mabe, Yoriko Watanabe, Makoto Yoshino, Toyojiro Matsuishi, Jun‐ichi Takanashi, Vorasuk Shotelersuk, Mustafa Tekin, Nobuhiko Ochi, Masaya Kubota, Naoko Ito, Kenji Ihara, Toshiro Hara, Hidefumi Tonoki, Tohru Ohta, Kayoko Saito, Mari Matsuo, Mari Urano, Takashi Enokizono, Astushi Sato, Hiroyuki Tanaka, Atsushi Ogawa, Takako Fujita, Yoko Hiraki, Sachiko Kitanaka, Yoichi Matsubara, Toshio Makita, Masataka Taguri, Mitsuko Nakashima, Yoshinori Tsurusaki, Hirotomo Saitsu, Ko‐ichiro Yoshiura, Naomichi Matsumoto, Norio Niikawa